Medical equipment and especially those classified as controlled technology, require special attention for compliance with the requirements related to sanitary regime, sanitary surveillance and Sanitary Registry, in this case called marketing permit.

Our firm has a group of biomedical engineers and health professionals with experience in the field who will be available to solve any concern ensuring an adequate management of the different requirements for import, manufacturing and / or marketing in Colombia.

We also advise them on compliance with a specific quality system for storing and packaging their products in accordance with Resolution 4002 of 2007. Consequently, our auditors offer in this case the possibility of preparing for the visit and later obtaining the Certificate of Conditions of Storage and Conditioning, necessary to obtain the Sanitary Registry.